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Synthesis of 1,2,4-triazole derivatives containing benzothiazoles as pharmacologically active molecule

机译:含有苯并噻唑作为药理活性分子的1,2,4-三唑衍生物的合成

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In attempt to make significant pharmacologically active molecule, we report here the synthesis and in vitro antimicrobial and antitubercular activity of various series of 3-(3-pyridyl)-5-(4-nitrophenyl)-4-(N-substituted-1,3-benzothiazol-2-amino)-4H-1,2,4-triazole. The antimicrobial activity of title compounds were examined against two Gram-positive bacteria (Staphylococcus aureus, Streptococcus pyogenes), two Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa), and three fungi (Candida albicans, Aspergillus niger, Aspergillus clavatus) using the broth microdilution method and antitubercular activity H37Rv using Lowenstein-Jensen agar method.
机译:为了尝试制造出重要的药理活性分子,我们在此报告了各种系列的3-(3-吡啶基)-5-(4-硝基苯基)-4-(N-取代-1)的合成以及体外抗微生物和抗结核活性, 3-苯并噻唑-2-氨基)-4H-1,2,4-三唑。检查了标题化合物对两种革兰氏阳性细菌(金黄色葡萄球菌,化脓性链球菌),两种革兰氏阴性细菌(大肠杆菌,铜绿假单胞菌)和三种真菌(白色念珠菌,黑曲霉,曲霉曲霉)的抗菌活性。 Lowenstein-Jensen琼脂法测定肉汤微量稀释法和抗结核活性H 37 Rv。

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